BETTER HEARING, INC. MODEL L-1 HEARING AID
K-Number: K971298 · 1997-07-23
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Device Summary
Frequently Asked Questions
What is the BETTER HEARING, INC. MODEL L-1 HEARING AID?
BETTER HEARING, INC. MODEL L-1 HEARING AID is a medical device that received FDA 510(k) clearance on 1997-07-23. The listed applicant is Better Hearing, Inc.. The 510(k) number is K971298.
When did BETTER HEARING, INC. MODEL L-1 HEARING AID receive FDA 510(k) clearance?
BETTER HEARING, INC. MODEL L-1 HEARING AID received FDA 510(k) clearance on 1997-07-23, under 510(k) number K971298.
Who is the listed applicant for BETTER HEARING, INC. MODEL L-1 HEARING AID?
The FDA 510(k) record lists Better Hearing, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BETTER HEARING, INC. MODEL L-1 HEARING AID?
The FDA product code for BETTER HEARING, INC. MODEL L-1 HEARING AID is ESD.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Better Hearing, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: ESD)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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